The novel aminoglycoside, ELX-02, permits CTNSW138X translational read-through and restores lysosomal cystine efflux in cystinosis von Brasell, Emma J, Chu, Lee Lee, Akpa, Murielle M, Eshkar-Oren, Idit, Alroy, Iris, Corsini, Rachel, Gilfix, Brian M, Yamanaka, Yojiro, Huertas, Pedro, Goodyer, Paul

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Utility of measuring serum or red blood cell folate in the era of folate fortification of flour von Gilfix, Brian M.

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Congenital disorders of glycosylation and the challenge of rare diseases von Gilfix, Brian M.

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Methionine dependence in tumor cells: The potential role of cobalamin and MMACHC von Sorin, Mark, Watkins, David, Gilfix, Brian M., Rosenblatt, David S.

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A new Capillary Zone Electrophoresis method for the screening of Congenital Disorders of Glycosylation (CDG) von Parente, Fabienne, Mew, Nicholas Ah, Jaeken, Jaak, Gilfix, Brian M.

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Congenital Disorders of Glycosylation: A Pipeline to Treatment? von Gilfix, Brian M.

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The Importance of Assessment of Function in the Era of In Silico Analysis von Gilfix, Brian M.

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Growth requirement for methionine in human melanoma-derived cell lines with different levels of MMACHC expression and methylation von Bauer, William G., Watkins, David, Zacharias, Caitlin, Gilfix, Brian M., Rosenblatt, David S.

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The Role of the ThyroSeq v3 Molecular Test in the Surgical Management of Thyroid Nodules in the Canadian Public Health Care Setting von Chen, Tanya, Gilfix, Brian M., Rivera, Juan, Sadeghi, Nader, Richardson, Keith, Hier, Michael P., Forest, Veronique-Isabelle, Fishman, Dina, Caglar, Derin, Pusztaszeri, Marc, Mitmaker, Elliot Jonathan, Payne, Richard J.

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Plasma phosphorylated tau181 outperforms [18F] fluorodeoxyglucose positron emission tomography in the identification of early Alzheimer disease von Quispialaya, Kely Monica, Therriault, Joseph, Aliaga, Antonio, Tissot, Cécile, Servaes, Stijn, Rahmouni, Nesrine, Karikari, Thomas K., Benedet, Andrea L., Ashton, Nicholas J., Macedo, Arthur C., Lussier, Firoza Z., Stevenson, Jenna, Wang, Yi‐Ting, Arias, Jaime Fernandez, Hosseini, Ali, Matsudaira, Takashi, Jean‐Claude, Bertrand, Gilfix, Brian M., Zimmer, Eduardo R., Soucy, Jean‐Paul, Pascoal, Tharick A., Gauthier, Serge, Zetterberg, Henrik, Blennow, Kaj, Rosa‐Neto, Pedro

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Biochemical analysis of patients with mutations in MTHFD1 and a diagnosis of methylenetetrahydrofolate dehydrogenase 1 deficiency von Bidla, Gawa, Watkins, David, Chéry, Céline, Froese, D. Sean, Ells, Courtney, Kerachian, Matin, Saskin, Avi, Christensen, Karen E., Gilfix, Brian M., Guéant, Jean-Louis, Rosenblatt, David S.

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Identification of Variants in Alpha-1-Antitrypsin by High Resolution Melting von Bidla, Gawa, Rosenblatt, David S, Gilfix, Brian M

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Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparison von Mattman, Andre, Gilfix, Brian M., Chen, Sharon Xuehui, DeMarco, Mari L., Kyle, Barry D., Parker, Michelle L., Agbor, Terence A., Jung, Benjamin, Selvarajah, Shamini, Barakauskas, Vilte E., Vaags, Andrea K., Estey, Mathew P., Nelson, Tanya N., Speevak, Marsha D.

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High resolution melting analysis of the MMAA gene in patients with cblA and in those with undiagnosed methylmalonic aciduria von Dempsey-Nunez, Laura, Illson, Margaret L., Kent, Jana, Huang, Qiuying, Brebner, Alison, Watkins, David, Gilfix, Brian M., Wittwer, Carl T., Rosenblatt, David S.

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Evaluation of the performance of multiple immunoassay diagnostic platforms on the National Microbiology Laboratory SARS-CoV-2 National Serology Panel von Dibernardo, Antonia, Toledo, Nikki PL, Robinson, Alyssia, Osiowy, Carla, Giles, Elizabeth, Day, Jacqueline, Robbin Lindsay, L, Drebot, Michael A, Booth, Timothy F, Pidduck, Tamara, Baily, Ashley, Charlton, Carmen L, Tipples, Graham, Kanji, Jamil N, Brochu, Gino, Lang, Amanda, Therrien, Christian, Bélanger-Collard, Mélina, Beaulac, Sylvie-Nancy, Gilfix, Brian M, Boivin, Guy, Hamelin, Marie-Ève, Carbonneau, Julie, Lévesque, Simon, Martin, Philippe, Finzi, Andrés, Gendron-Lepage, Gabrielle, Goyette, Guillaume, Benlarbi, Mehdi, Gasser, Romain, Fortin, Claude, Martel-Lafferrière, Valérie, Lavoie, Myriam, Guérin, Renée, Haraoui, Louis-Patrick, Renaud, Christian, Jenkins, Craig, O'Brien, Sheila F, Drews, Steven J, Conrod, Valerie, Tran, Vanessa, Awrey, Bill, Scheuermann, Robert, DuPuis, Alan, Payne, Anne, Warszycki, Casey, Girardin, Roxie, Lee, William, Zahariadis, George, Jiao, Lei, Needle, Robert, Cordenbach, James, Zaharatos, Jerry, Taylor, Kellee, Teltscher, Marty, Miller, Matthew, Elsherif, May, Robertson, Peter, Robinson, Jason L

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Apolipoprotein E4 Allele as a Predictor of Cholinergic Deficits and Treatment Outcome in Alzheimer Disease von Poirier, J, Delisle, M C, Quirion, R, Aubert, I, Farlow, M, Lahiri, D, Hui, S, Bertrand, P, Nalbantoglu, J, Gilfix, B M, Gauthier, S

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Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis von Awan, Zuhier, Aljenedil, Sumayah, Rosenblatt, David S, Cusson, Jean, Gilfix, Brian M, Genest, Jacques

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High resolution melting analysis of the MMAB gene in cblB patients and in those with undiagnosed methylmalonic aciduria von Illson, Margaret L., Dempsey-Nunez, Laura, Kent, Jana, Huang, Qiuying, Brebner, Alison, Raff, Michael L., Watkins, David, Gilfix, Brian M., Wittwer, Carl T., Rosenblatt, David S.

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Comment on Complications Following Antidotal Use of Intravenous Lipid Emulsion Therapy (Levine et al., J Med Toxicol 2013) von Grunbaum, Ami M., Gosselin, Sophie, Gilfix, Brian M., Blank, David W.

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Vitamin B12 and homocysteine von Gilfix, Brian M

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